Profiling microRNAs in lung tissue from pigs infected with Actinobacillus pleuropneumoniae

Agnieszka Podolska1, Christian Anthon, Mads Bak

  • 1Department of Veterinary Clinical and Animal Sciences, Section of Anatomy, Cell Biology, Genetics and Bioinformatics, University of Copenhagen, Faculty of Health and Medical Sciences, Copenhagen, Denmark.

BMC Genomics
|September 8, 2012
PubMed
Abstract

Insights

This study identifies microRNAs (miRNAs) in pigs affected by Actinobacillus pleuropneumoniae lung infections. It reveals significant differences in miRNA expression, highlighting potential roles in the immune response to bacterial pathogens.

Area of Science:

  • Veterinary Science
  • Molecular Biology
  • Immunology

Background:

  • MicroRNAs (miRNAs) are crucial regulators in mammalian development and disease, but their functions in porcine infectious diseases are poorly understood.
  • Actinobacillus pleuropneumoniae (APP) causes severe, often fatal, lung infections in pigs, with limited knowledge of the host's microRNA involvement.
  • Understanding miRNA roles in APP infection is vital for developing new therapeutic strategies.

Purpose of the Study:

  • To investigate the role of microRNAs in porcine lung tissue during Actinobacillus pleuropneumoniae infection.
  • To identify and characterize differentially expressed miRNAs in response to bacterial infection.
  • To provide insights into the host's immune and inflammatory responses at the molecular level.

Main Methods:

  • Small RNA deep sequencing was performed on unaffected and necrotic lung tissues from pigs infected with APP.
  • Identification of conserved and novel microRNAs in porcine lung tissue.
  • Differential expression analysis of identified microRNAs.

Main Results:

  • 169 conserved and 11 novel microRNAs were identified in the pig.
  • Significant differential expression of miRNAs was observed, with 17 up-regulated and 12 down-regulated in necrotic tissue.
  • Specific miRNAs, including miR-155, miR-664-5p, miR-451, and miR-15a, were highlighted for their potential roles in the innate immune response to bacterial infection.

Conclusions:

  • This study presents the first evidence of altered miRNA profiles in porcine lungs infected with a bacterial pathogen.
  • The findings expand the annotation of porcine miRNAs and offer insights into their regulatory functions in bacterial-induced immune and inflammatory responses.
  • The identified miRNAs represent potential biomarkers and therapeutic targets for Actinobacillus pleuropneumoniae infections.